Transmembrane receptor Regulation

Desai, D. M., Sap, J., Schlessinger, J. et al. Ligand-mediated negative regulation of a chimeric transmembrane receptor tyrosine phosphatase. Cell 73 541-554,1993. 

The structural analysis of membrane-associated peptides comprises two steps (a) the elucidation of the three-dimensional fold of the peptide and (b) the determination of the membrane-peptide interface. We will use our results gained for the 36 amino acid residue neuropeptide Y (NPY) [83] to demonstrate the approaches that can be used. NPY regulates important pharmacological functions such as blood pressure, food intake or memory retention and hence has been subject of many investigations (for a review see Ref. [84]). It targets the so-called Y receptors that belong to the class of seven transmembrane receptors coupled to G-proteins (GPCRs). 

Hawkes C, Jhamandas JH, Harris K, Fu J, Mac Donald RG, et al. 2006. Single transmembrane domain insulin-like growth factor-II/mannose-6-phosphate receptor regulates central cholinergic function by activating a G-protein-sensi-tive, protein kinaseC-dependent pathway. J Neurosci 26 585-596. 

Fig. 3.6. Principles of signal transduction by transmembrane receptors and nuclear receptors, a) transmembrane receptors receive the signal on the cell surface and convert it into an intracellular signal that can be passed on until it reaches the nucleus, b) In signal transduction via nuclear receptors the hormone enters the cell and binds the receptor either in the cytosol (R) or nucleus (R ). Nuclear receptors act as nuclear transcription factors that bind specific DNA elements (HRE hormone responsive element) found in the promotor region of regulated genes to control their transcription rate.

Phospholipase C, which occurs in different subtypes in the cell, is a key enzyme of phosphatide inositol metabohsm (for cleavage specificity, see Fig. 5.24). Two central signaling pathways regulate phosphohpase C activity of the cell in a positive way (Fig. 6.4). Phospholipases of type CP (PL-CP) are activated by G-proteins and are thus linked into signal pathways starting from G-protein-coupled receptors. Phosphohpases of type Y (PL-Cy), in contrast, are activated by transmembrane receptors with intrinsic or associated tyrosine kinase activity (see Chapter 8, Chapter 10). The nature of the extracellular stimuli activated by the two major reaction pathways is very diverse (see Fig 6.4), which is why the phosphohpase C activity of the cell is subject to multiple regulation. 

Fig. 6.4. Formation and function of diacylglycerol and Ins(l,4,5)P3. Formation of diacylglycerol (DAG) and Ins(l,4,5)P3 is subject to regulation by two central signaling pathways, which start from transmembrane receptors with intrinsic or associated tyrosine kinase activity (see Chapters 8 11) or from G-protein-coupled receptors. DAG activates protein kinase C (PKC, see Chapter 7), which has a regulatory effect on ceU proliferation, via phosphorylation of substrate proteins. Ins(l,4,5)P3 binds to corresponding receptors (InsPs-R) and induces release of Ca from internal stores. The membrane association of DAG, PtdIns(3,4)P2 and PL-C is not shown here, for clarity.

Ion channels can also be opened by a direct effect of an activated G-protein. In this case, the extracellular messenger binds to a G-protein-coupled transmembrane receptor and activates a heterotrimeric G-protein. This acts directly on an ion channel and regulates its open state. 

Figure 19-5 Schematic representation of an important chemotactic system of E. coli, S. typhimurium, and other bacteria. The transmembrane receptor activates the autokinase CheA, which transfers its phospho group to proteins CheY and CheB to form CheY-P and CheB-P. CheY-P regulates the direction of rotation of the flagella, which are distributed over the bacterial surface. CheR is a methyltransferase which methylates glutamate carboxyl groups in the receptor and modulates the CheA activity. CheZ is a phosphatase and CheB-P a methylesterase.

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